Evidence map›Paper›PMID 33690724›Full record

Observational studyPloS one2021

Automatic real-time analysis and interpretation of arterial blood gas sample for Point-of-care testing: Clinical validation.

Sancho Rodríguez-Villar, Paloma Poza-Hernández, Sascha Freigang, Idoia Zubizarreta-Ormazabal, Daniel Paz-Martín, Etienne Holl, Osvaldo Ceferino Pérez-Pardo, María Sherezade Tovar-Doncel, Sonja Maria Wissa, Bonifacio Cimadevilla-Calvo and 8 more

Open access · goldAbstract readMulticenter StudyObservational Study
In one paragraph

Observational study in PloS one, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.9field-weighted citation impact, top 15% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 20 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

18 authors at 7 institutions in 4 countries.

Sancho Rodríguez-VillarCritical Care Department, King´s College Hospital, London, United Kingdom.ORCID 0000-0002-8976-9101
Paloma Poza-HernándezHospital Virgen de la Salud, Servicio de Anestesia y Reanimación, Surgical Intensive Care Unit, Complejo Hospitalario de Toledo, Toledo, Spain.
Sascha FreigangDepartment of Neurosurgery, Neurosurgical Intensive Care Unit, Medical University of Graz, Graz, Austria.
Idoia Zubizarreta-OrmazabalMarqués de Valdecilla University Hospital (HUMV), Servicio de Anestesia y Reanimación, Santander, Cantabria, Spain.
Daniel Paz-MartínHospital Virgen de la Salud, Servicio de Anestesia y Reanimación, Surgical Intensive Care Unit, Complejo Hospitalario de Toledo, Toledo, Spain.
Etienne HollDepartment of Neurosurgery, Neurosurgical Intensive Care Unit, Medical University of Graz, Graz, Austria.
Osvaldo Ceferino Pérez-PardoMarqués de Valdecilla University Hospital (HUMV), Servicio de Anestesia y Reanimación, Santander, Cantabria, Spain.
María Sherezade Tovar-DoncelHospital Virgen de la Salud, Servicio de Anestesia y Reanimación, Surgical Intensive Care Unit, Complejo Hospitalario de Toledo, Toledo, Spain.
Sonja Maria WissaDepartment of Neurosurgery, Neurosurgical Intensive Care Unit, Medical University of Graz, Graz, Austria.
Bonifacio Cimadevilla-CalvoMarqués de Valdecilla University Hospital (HUMV), Servicio de Anestesia y Reanimación, Santander, Cantabria, Spain.
Guillermo Tejón-PérezMarqués de Valdecilla University Hospital (HUMV), Servicio de Anestesia y Reanimación, Santander, Cantabria, Spain.
Ismael Moreno-FernándezMedical Software Specialist at Madrija Company, Toledo, Spain.
Alejandro Escario-MéndezMedical Software Specialist at Madrija Company, Toledo, Spain.
Juan Arévalo-SerranoInternal Medicine Department, Príncipe de Asturias Hospital, Alcalá de Henares, Madrid, Spain.
Antonio ValentínDepartment of Basic and Clinical Neuroscience, Institute of Psychiatry, Psychology & Neuroscience (IoPPN) Academic Neuroscience Centre, London, United Kingdom.
Bruno Manuel Do-ValeCritical Care Department, Centro Hospitalar Universitário do Porto (CHUP), Porto, Portugal.ORCID 0000-0003-1867-0849
Helen Marie FletcherExecutive Nursing Department, King´s College Hospital, London, United Kingdom.
Jesús Medardo Lorenzo-FernándezExternal Consultant, Ingeniero de Caminos, Canales y Puertos e Ingeniero Técnico de Obras Públicas.
Marqués de Valdecilla University Hospital · ESHospital Virgen de la Salud · ESMedical University of Graz · ATKing's College Hospital · GBCentro de Estudios y Experimentación de Obras Públicas · ESCentro Hospitalar do Porto · PTHospital Universitario Príncipe de Asturias · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPoint-of-care arterial blood gas (ABG) is a blood measurement test and a useful diagnostic tool that assists with treatment and therefore improves clinical outcomes. However, numerically reported test results make rapid interpretation difficult or open to interpretation. The arterial blood gas algorithm (ABG-a) is a new digital diagnostics solution that can provide clinicians with real-time interpretation of preliminary data on safety features, oxygenation, acid-base disturbances and renal profile. The main aim of this study was to clinically validate the algorithm against senior experienced clinicians, for acid-base interpretation, in a clinical context.

methodsWe conducted a prospective international multicentre observational cross-sectional study. 346 sample sets and 64 inpatients eligible for ABG met strict sampling criteria. Agreement was evaluated using Cohen's kappa index, diagnostic accuracy was evaluated with sensitivity, specificity, efficiency or global accuracy and positive predictive values (PPV) and negative predictive values (NPV) for the prevalence in the study population.

resultsThe concordance rates between the interpretations of the clinicians and the ABG-a for acid-base disorders were an observed global agreement of 84,3% with a Cohen's kappa coefficient 0.81; 95% CI 0.77 to 0.86; p < 0.001. For detecting accuracy normal acid-base status the algorithm has a sensitivity of 90.0% (95% CI 79.9 to 95.3), a specificity 97.2% (95% CI 94.5 to 98.6) and a global accuracy of 95.9% (95% CI 93.3 to 97.6). For the four simple acid-base disorders, respiratory alkalosis: sensitivity of 91.2 (77.0 to 97.0), a specificity 100.0 (98.8 to 100.0) and global accuracy of 99.1 (97.5 to 99.7); respiratory acidosis: sensitivity of 61.1 (38.6 to 79.7), a specificity of 100.0 (98.8 to 100.0) and global accuracy of 98.0 (95.9 to 99.0); metabolic acidosis: sensitivity of 75.8 (59.0 to 87.2), a specificity of 99.7 (98.2 to 99.9) and a global accuracy of 97.4 (95.1 to 98.6); metabolic alkalosis sensitivity of 72.2 (56.0 to 84.2), a specificity of 95.5 (92.5 to 97.3) and a global accuracy of 93.0 (88.8 to 95.3); the four complex acid-base disorders, respiratory and metabolic alkalosis, respiratory and metabolic acidosis, respiratory alkalosis and metabolic acidosis, respiratory acidosis and metabolic alkalosis, the sensitivity, specificity and global accuracy was also high. For normal acid-base status the algorithm has PPV 87.1 (95% CI 76.6 to 93.3) %, and NPV 97.9 (95% CI 95.4 to 99.0) for a prevalence of 17.4 (95% CI 13.8 to 21.8). For the four-simple acid-base disorders and the four complex acid-base disorders the PPV and NPV were also statistically significant.

conclusionsThe ABG-a showed very high agreement and diagnostic accuracy with experienced senior clinicians in the acid-base disorders in a clinical context. The method also provides refinement and deep complex analysis at the point-of-care that a clinician could have at the bedside on a day-to-day basis. The ABG-a method could also have the potential to reduce human errors by checking for imminent life-threatening situations, analysing the internal consistency of the results, the oxygenation and renal status of the patient.

Indexed as

Acid-Base EquilibriumAcid-Base ImbalanceAcidosisAdolescentAdultAgedAlgorithmsAlkalosisAlkalosis, RespiratoryArterial PressureBlood Gas AnalysisChildChild, PreschoolCross-Sectional StudiesFemaleHumans

Identifiers

PMID33690724
PMCPMC7946183
OpenAlexW3135063454

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.